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Achromatopsia
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Alagille syndrome
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Vascular Malformations SuperPanel
Vitamin metabolism disorders
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Version
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2.0
1.88
Gene or Genomic Entity Name
VMA22
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07 Jun 2026
Congenital Disorders of Glycosylation v2.0
VMA22
Gene symbol changed from CCDC115 to VMA22 during gene set migration (ENSG00000136710 -> ENSG00000136710)